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排序方式: 共有172条查询结果,搜索用时 15 毫秒
31.
Toshio Ito Nobuya Tomiyoshi Koki Nakamura Shizuo Azuma Makoto Izawa Fumio Maruyama Mitsutoshi Yanagiya Haruhisa Shirahama Takeshi Matsumoto 《Tetrahedron》1984,40(1):241-255
The total synthesis of dl-coriolin has been achieved in a stereoselective way. The key tricyclic intermediate was synthesized from dicyclopentadiene through a route which involved an SN2 reaction at a neopentylic position. 相似文献
32.
33.
An efficient algorithm is proposed for finding all solutions of systems of n nonlinear equations. This algorithm is based on interval analysis and a new strategy called LP narrowing. In the LP narrowing strategy, boxes (n-dimensional rectangles in the solution domain) containing no solution are excluded, and boxes containing solutions are narrowed so that no solution is lost by using linear programming techniques. Since the LP narrowing is very powerful, all solutions can be found very efficiently. By numerical examples, it is shown that the proposed algorithm could find all solutions of systems of 5000-50,000 nonlinear equations in practical computation time. 相似文献
34.
A series of "organic chemical hydrides" such as cyclohexane, methylcyclohexane, cyclohexene, 2-propanol, and cyclohexanol were applied to the direct PEM fuel cell. High performances of the PEM fuel cell were achieved by using cyclohexane (OCV = 920 mV, PD(max) = 15 mW cm(-2)) and 2-propanol (OCV = 790 mV, PD(max) = 78 mW cm(-2)) as fuels without CO(2) emissions. The rates of fuel crossover for cyclohexane, 2-propanol, and methanol were estimated, and the rates of fuel permeation of cyclohexane and 2-propanol were lower than that of methanol. Water electrolysis and electro-reductive hydrogenation of acetone mediated by PEM were carried out and formation of 2-propanol in cathode side was observed. This system is the first example of a "rechargeable" direct fuel cell. 相似文献
35.
Tetsu Tsubogo Yuichiro Kano Koki Ikemoto Yasuhiro Yamashita Shū Kobayashi 《Tetrahedron: Asymmetry》2010,21(9-10):1221-1225
The first catalytic asymmetric 1,4-addition reactions of azlactones with acrylic esters have been developed. A chiral coordinative calcium catalyst was found to be effective for these reactions, and the desired 1,4-adducts were obtained in good yields and enantioselectivities. The product was converted to the corresponding α-alkylated glutamic acid by acid hydrolysis. 相似文献
36.
Yukihiko Nagase Norio Suzuki Hitoshi Yamauchi Sunyong Kim Koki Wada Hidetosh Arima Fumitoshi Hirayama Kaneto Uekama 《Journal of inclusion phenomena and macrocyclic chemistry》2002,44(1-4):107-110
The interaction of ebselen, 2-phenyl-1,2-benzisoselenazol-3(2H)-one, a novel neuroprotective agent, with cyclodextrins (CyDs) in aqueous solution was studied by the solubility method and spectroscopic methods. The ability of sulfobutyl ether -CyD (SBE7--CyD, average degree of substitution= 6.2) to solubilize ebselen was greater, and its stability constant (> 2000 M-1) was significantly higher than those (< 1000 M-1) of other CyD complexes employed. The stability constant of the complexes rose as hydrophobicity of the substituents of CyDs increased, whereas it was negligibly affected by change in ionic strength of the medium, indicating a significant contribution of hydrophobic interaction in the complexation. SBE7--CyD gave positive and negative CD bands at around 320 and 350 nm, respectively, indicating that the guest is embedded in the asymmetric locus of the CyD cavity. 1H-NMR spectroscopic studies suggested that the mono-substituted benzene ring of ebselen is preferably included in the cavity of SBE7--CyD. The results indicate that SBE7--CyD is useful as a solubilizing agent for ebselen. 相似文献
37.
Nobutoshi Kiba Ayumi Koga Masaki Tachibana Kazue Tani Hitoshi Koizumi Tetsuo Koyama Akira Yamamura Kunio Matsumoto Tohru Okuda Koki Yokotsuka 《Analytical sciences》2006,22(1):95-98
A chemiluminometric flow injection analytical system for the quantitation of L-histidine is described. Histidine oxidase (EC 1.4.3.-) from Brevibacillus borstelensis KAIT-B-022 was immobilized on tresylated poly(vinyl alcohol) beads and packed into a stainless-steel column. The hydrogen peroxide produced was detected chemiluminometrically by a flowthrough sensor containing immobilized peroxidase (EC 1.1 1.1.7). The maximum sample throughput was 10 h(-1). The calibration graph was linear from 0.05 to 5 mM; the detection limit (signal to noise ratio = 3) was 0.01 mM. The activity of immobilized histidine oxidase reduced to 65% of the initial value after 350 injections. The system was applied to the determination of L-histidine in fish meat, such as salmon, tunny, bonito, and mackerel. 相似文献
38.
Koki Tsukamoto Hideaki Shimizu Takashi Ishida Yutaka Akiyama Nobuyuki Nukina 《Journal of Molecular Structure》2006,778(1-3):85-95
Polyglutamine (polyQ) diseases, including Huntington’s disease (HD), are caused by expansion of polyQ-encoding repeats within otherwise unrelated gene products. The aggregation mechanism of polyQ diseases, the inhibition mechanism of Congo red, and the alleviation mechanism of trehalose were proposed here based on quantum chemical calculations and molecular dynamics simulations. The calculations and simulations revealed the following. The effective molecular bonding is between glutamine (Gln) and Gln (Gln + Gln), between Gln and Congo red (Gln + Congo red), and between Gln and trehalose (Gln + trehalose). The bonding strength is −13.1 kcal/mol for Gln + Gln, −24.4 kcal/mol for Gln + Congo red, and −12.0 kcal/mol for Gln + trehalose. In the polyQ region, both the number of intermolecular Gln + Gln formations and the total calories generated by the Gln + Gln formation are proportional to the number of repetitions of Gln. We propose an aggregation mechanism whose heat generated by the intermolecular Gln + Gln formation causes the pathogeny of polyQ disease. In our aggregation mechanism, this generated heat collapses the host protein and promotes fibrillogenesis. Without contradiction, our mechanism can explain all the experimental results reported to date. Our mechanism can also explain the inhibition mechanism by Congo red as an inhibitor of polyglutamine-induced protein aggregation and the alleviation mechanism by trehalose as an alleviator of that aggregation. The inhibition mechanism by Congo red is explained by the strong interaction with Gln and by the characteristic structure of Congo red. 相似文献
39.
Summary The biochemical functions of uridine-diphosphate-amino-sugar conjugates are largely unknown. As a first step to investigate
their biological roles in glycolysis of higher organisms, bovine heart muscle, which metabolizes large quantities of glycogen,
was assayed for uridine-diphosphate-hexosamine. A low molecular mass ultrafiltrate was prepared from the methanolsoluble fraction
of a beef heart homogenate, and the fraction was further purified using anion-exchange and reverse-phase HPLC. Samples were
analyzed by two HPLC methods; anion-exchange in borate buffer and reverse-phase ion-pair chromatography. One newly established
technique employing phenylthiocarbamoyl labelled uridine-diphosphate-hexosamine also was used selectively to separate uridine-diphosphate-hexosamine
from other uridine-diphosphate-sugars. Hydrolysate of purified sample was classified further according to molecular structure.
As a result, phenylthiocarbamoyl labelled HPLC is suitable and easy for the detection of uridine-diphosphate-hexosamine and
its derivatives. 相似文献
40.
Koki Yamaguchi 《Tetrahedron letters》2005,46(7):1087-1090
Dimethyl 5-hydroxy-2-oxo-4,5-diphenylcyclopent-3-ene-1,3-dicarboxylate (1a) forms relatively stable inclusion complexes with compounds having 1,2-diaminoethane moiety. 相似文献